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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2260 | Glenvastatin |
Novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor
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| DCC2259 | glaziovianin A |
Novel inhibitor of the cell cycle progression in M-phase; Inhibotor of endosome maturation
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| DCC2258 | Gkm001 |
First-in-class liver-selective glucokinase activator for the treatment of type 2 diabetes
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| DCC2257 | Gka-71 |
Novel and potent glucokinase activator (GKA)
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| DCC2256 | Gka-22 |
Novel Allosteric Activator of Human Glucokinase in the Absence of Glucose
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| DCC2255 | Gk-667 |
Novel water solubile prodrug of ICRF-193, penetrating into NVCMs, reaching intracellular concentrations sufficient to induce cytoprotective effects against ANT toxicity
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| DCC2254 | Gk-136901 |
First-in-Class, Potent, and Orally Bioavailable NADPH Oxidase Isoform 4 (Nox4) Inhibitor
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| DCC2253 | Ginnalin A |
Natural Activator of the Nrf2-Regulated Antioxidant Defense System in SH-SY5Y Cells, Binding to the Subpockets of Keap1 Kelch Domain
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| DCC2252 | Ginkgonitroside |
Natural suppressor of mesenchymal stem cell (MSC) differentiation
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| DCC2250 | Gif-0856-r |
Novel suppressor of endoplasmic reticulum (ER) stress and oxidative stress, preventing protein aggregate accumulation in vitro and in cultured hippocampal HT22 neuronal cells, as well as glutamate-induced oxytosis and erastin-induced ferroptosis
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| DCC2249 | Gif-0854-r |
Novel suppressor of endoplasmic reticulum (ER) stress and oxidative stress, preventing protein aggregate accumulation in vitro and in cultured hippocampal HT22 neuronal cells, as well as glutamate-induced oxytosis and erastin-induced ferroptosis
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| DCC2248 | Gidazepam |
Potent mitochondrial benzodiazepine receptors (MBRs) ligand; Prodrug for its active metabolite bromo-nordazepam
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| DCC2247 | Gic-1001 |
Novel oral anti-nociceptive agent, showing peripheral opioid agonistic activity and hydrogen sulphide-releasing capacity
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| DCC2246 | Gi261520a |
Potent EGFR/erbB2 dual inhibitor
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| DCC2245 | Gi-129471 |
Metalloproteinase inhibitor, specifically blocking TNF-alpha secretion both in vitro and in vivo
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| DCC2244 | Ghsr Inverse Agonist 29 |
Novel nonpeptidic inverse agonist of the Ghrelin Receptor (GHSR)
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| DCC2243 | G-glu-glu |
Endogenous dipeptide, activating N-methyl-D-aspartate receptors
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| DCC2241 | Geopyxin F |
Natural non-covalent NRF2 activator, activating NRF2 in A KEAP1-dependent but Cys151-independent manner, conferring greater protection than a Cys151-dependent analog, geopyxin C
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| DCC2240 | Geopyxin C |
Natural covalent Cys151-dependent NRF2 activator
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| DCC2239 | Geneseroline |
Metabolite of ganstigmine, a novel acetylcholinesterase inhibitor
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| DCC2238 | Genaconazole |
Novel antifungal agent
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| DCC2237 | Geiparvarin |
MAO inhibitor
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| DCC2236 | Gebr-7b |
Novel Phosphodiesterase 4D (PDE4D) Inhibitor
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| DCC2235 | Gdk-100017 |
Inhibitor of the Wnt/beta-catenin signaling pathway, suppressing cell proliferation and enhancing radiosensitivity in A549/Wnt2 cells.
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| DCC2233 | Gdc-0917 |
Novel SMAC mimetic and IAP antagonist
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| DCC2232 | Gdc-0834 |
Novel Bruton's tyrosine kinase (BTK) inhibitor
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| DCC2231 | Gdc-0575 Dihydrochloride |
Novel potent, selective and orally bioavailable Chk1 inhibitor
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| DCC2230 | Gdc0575 |
Novel highly-selective oral checkpoint kinase 1 (Chk1) inhibitor
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| DCC2229 | Gcs Inhibitor Bz1 |
Novel glucosylceramide synthase (GCS) inhibitor, rescuing lysosomal deficits, α-synuclein pathology and neuron toxicity
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| DCC2228 | Gcc5694a |
Novel Potent and Selective Sodium Glucose Co-Transporter 2 (SGLT2) Inhibitor for the Treatment of Type 2 Diabetes
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